TY - JOUR
T1 - Hydrogen production from biomass via a near-room temperature aqueous-phase tandem catalytic approach
AU - Geng, Yiqi
AU - Xue, Wenhua
AU - Ye, Jian
AU - Zhang, Ruilong
AU - Johnravindar, Davidraj
AU - Zhao, Jun
N1 - Funding Information:
This work was supported by the Hong Kong Innovation and Technology Fund (Ref. ITS-065-22MX) and Environment and Conservation Fund (Ref. 2021-127).
Publisher Copyright:
© 2024 Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2025/1/15
Y1 - 2025/1/15
N2 - Hydrogen is pivotal for the shift towards cleaner energy systems, prompting the need for sustainable, efficient green hydrogen production methods. This study introduced a one-pot hydrogen production process from biomass through a glucose-formic acid-hydrogen pathway. Using hydrogen peroxide as an oxidant, the optimized MgO nanoflowers catalyst yielded an impressive 81.17 % conversion of glucose to formic acid. Investigation into the catalytic mechanism showed that MgO crystallinity markedly influences catalytic performance, with simulation calculations indicating superior kinetic and thermodynamic benefits in α-scission reactions, enhancing formic acid generation. Direct catalytic dehydrogenation of the crude formic acid solution yielded 88.45 % hydrogen from glucose at nearly ambient temperature within an hour, equivalent to 580 mL H2/g glucose. Extending this catalytic approach, hydrogen was produced from food waste through acid-catalyzed hydrolysis to glucose, followed by oxidation and dehydrogenation, demonstrating an efficient and sustainable route for green hydrogen production from biomass and food waste.
AB - Hydrogen is pivotal for the shift towards cleaner energy systems, prompting the need for sustainable, efficient green hydrogen production methods. This study introduced a one-pot hydrogen production process from biomass through a glucose-formic acid-hydrogen pathway. Using hydrogen peroxide as an oxidant, the optimized MgO nanoflowers catalyst yielded an impressive 81.17 % conversion of glucose to formic acid. Investigation into the catalytic mechanism showed that MgO crystallinity markedly influences catalytic performance, with simulation calculations indicating superior kinetic and thermodynamic benefits in α-scission reactions, enhancing formic acid generation. Direct catalytic dehydrogenation of the crude formic acid solution yielded 88.45 % hydrogen from glucose at nearly ambient temperature within an hour, equivalent to 580 mL H2/g glucose. Extending this catalytic approach, hydrogen was produced from food waste through acid-catalyzed hydrolysis to glucose, followed by oxidation and dehydrogenation, demonstrating an efficient and sustainable route for green hydrogen production from biomass and food waste.
KW - Biomass conversion
KW - Biorefinery
KW - Glucose
KW - Heterogeneous catalysis
KW - Magnesium oxide
UR - http://www.scopus.com/inward/record.url?scp=85212962805&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2024.158846
DO - 10.1016/j.cej.2024.158846
M3 - Journal article
AN - SCOPUS:85212962805
SN - 1385-8947
VL - 504
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 158846
ER -